Kolehmainen Reija E, Tiirola Marja, Puhakka Jaakko A
Department of Chemistry and Bioengineering, Tampere University of Technology, Tampere, Finland.
Water Res. 2008 Nov;42(17):4525-37. doi: 10.1016/j.watres.2008.07.039. Epub 2008 Aug 9.
Artificial groundwater recharge (AGR) is used in the drinking water industry to supplement groundwater resources and to minimise the use of chemicals in water treatment. This study analysed the spatial and temporal changes of microbial communities in AGR using two test systems: a nutrient-amended fluidized-bed reactor (FBR) and a sand column. Structural changes in the feed lake water (Lake Roine), FBR, and sand column bacterial communities were determined by denaturing gradient gel electrophoresis (DGGE) and the length heterogeneity analysis of amplified 16S rRNA genes (LH-PCR). Two clone libraries were created to link the LH-PCR results to the dominant bacterial groups. The lake water bacterial community was relatively stable, with three bands dominating in all LH-PCR products. The most dominant fragment accounted for up to 72% and was derived from Actinobacteria. Based on the clone libraries and LH-PCR data, Actinobacteria also dominated in the unattached bacterial community of the FBR, whereas several Proteobacterial groups were more abundant on the FBR carrier particles. In the stabilised AGR system a major change in the community structure of the lake water bacteria took place during passage within the first 0.6m in the sand column as the community composition shifted from Actinobacteria-dominated populations to a diverse, mainly Proteobacterial communities. Concurrently, most of the dissolved organic carbon (DOC) was removed at this stage. In summary, the study showed that the make-up of microbial communities in experimental AGR systems responded to changes in their environment. LH-PCR showed potential as a method to determine microbial community dynamics in long-term studies at real-scale AGR sites. This is the first step to provide data on microbial community dynamics in AGR for drinking water production.
人工地下水回灌(AGR)在饮用水行业中用于补充地下水资源,并尽量减少水处理过程中化学药剂的使用。本研究使用两个测试系统分析了AGR中微生物群落的时空变化:一个添加营养物质的流化床反应器(FBR)和一个砂柱。通过变性梯度凝胶电泳(DGGE)和扩增的16S rRNA基因长度异质性分析(LH-PCR)确定了进水湖水(罗伊内湖)、FBR和砂柱细菌群落的结构变化。创建了两个克隆文库,以将LH-PCR结果与优势细菌类群联系起来。湖水细菌群落相对稳定,在所有LH-PCR产物中,有三条带占主导地位。最主要的片段占比高达72%,来源于放线菌。基于克隆文库和LH-PCR数据,放线菌在FBR的非附着细菌群落中也占主导地位,而几个变形菌门类群在FBR载体颗粒上更为丰富。在稳定的AGR系统中,湖水细菌群落结构在砂柱中最初的0.6米内发生了重大变化,群落组成从以放线菌为主的种群转变为多样的、主要以变形菌为主的群落。同时,大部分溶解有机碳(DOC)在这个阶段被去除。总之,该研究表明,实验性AGR系统中微生物群落的组成对其环境变化做出了响应。LH-PCR显示出作为一种在实际规模的AGR场地长期研究中确定微生物群落动态的方法的潜力。这是为饮用水生产提供AGR中微生物群落动态数据的第一步。